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Professor Kate Schroder
Professor

Kate Schroder

Email: 
Phone: 
+61 7 334 62058

Overview

Background

Professor Kate Schroder heads the Inflammasome Laboratory and is Director of the Centre for Inflammation and Disease Research at the Institute for Molecular Bioscience (IMB), University of Queensland, as an NHMRC Leadership Fellow. Kate’s graduate studies defined novel macrophage activation mechanisms and her subsequent postdoctoral research identified surprising inter-species divergence in the inflammatory programs of human versus mouse macrophages. As an NHMRC CJ Martin Fellow in Switzerland, Kate trained with the pioneer of inflammasome biology, Jürg Tschopp. The IMB Inflammasome Laboratory, which Kate heads, investigates the molecular mechanisms governing inflammasome activity and caspase activation, the cellular mediators of inflammasome-dependent inflammation, and mechanisms of inflammasome inhibition by cellular pathways and small molecule inhibitors.

Kate is a co-inventor on patents for small molecule inhibitors of the NLRP3 inflammasome, currently under commercialisation by Inflazome Ltd. Inflazome Ltd was recently acquired by Roche in a landmark deal – one of the largest in Australian and Irish biotech history. The acquisition gives Roche full rights to Inflazome’s portfolio of inflammasome inhibitors. Two of the company’s drug candidates are in clinical trials for the treatment of debilitating conditions such as cardiovascular disease, arthritis and neurodegenerative diseases such as Parkinson’s, Alzheimer’s and motor neuron disease.

Kate has authored more than 140 publications, featuring in journals such as Science, Cell, Nature Genetics, Nature Medicine, Nature Chemical Biology, Journal of Experimental Medicine and PNAS USA, and her work has been cited more than 35,000 times. Kate is an Editorial Board Member for international journals including Science Signaling, Clinical and Translational Immunology and Cell Death Disease. She is the recipient of the 2022 Women in Technology Excellence in Science Award, 2020 Nancy Mills Award for Women in Science, 2019 ANZSCDB Emerging Leader Award, 2019 Merck Research Medal, 2014 Milstein Young Investigator Award, 2013 Tall Poppy Award, 2012 Gordon Ada Career Award, 2010 QLD Premier’s Postdoctoral Award, and the 2008 Society for Leukocyte Biology’s Dolph Adams Award.

INFLAMMASOME LABORATORY RESEARCH

During injury or infection, our body’s immune system protects us by launching inflammation. But uncontrolled inflammation drives diseases such as gout, diabetes, neurodegenerative disease and cancer. The Inflammasome Lab is defining the molecular and cellular processes of inflammation. We seek to unravel the secrets of inflammasomes – protein complexes at the heart of inflammation and disease – to allow for new therapies to fight human diseases.

The Inflammasome Laboratory integrates molecular and cell biology approaches with in vivo studies to gain a holistic understanding of inflammasome function during infection, and inflammasome dysfunction in human inflammatory disease. Current research interests include the molecular mechanisms governing inflammasome activity and caspase activation, the cellular mediators of inflammasome-dependent inflammation, and inflammasome suppression by autophagy and small molecule inhibitors.

Availability

Professor Kate Schroder is:
Available for supervision
Media expert

Qualifications

  • Bachelor (Honours) of Science (Advanced), The University of Queensland
  • Doctor of Philosophy, The University of Queensland

Research impacts

Our research focuses on understanding how immune cells launch healthy inflammation to fight infection and unhealthy inflammation to promote disease. By understanding exactly how the body fights infection, we can help identify new drug targets or vaccines to combat infectious disease, which causes 13 million deaths globally each year. By understanding how unhealthy inflammation is initiated, we may also be able to design new strategies for the treatment of common diseases such as cancer, gout and diabetes.

Works

Search Professor Kate Schroder’s works on UQ eSpace

165 works between 2001 and 2024

81 - 100 of 165 works

2017

Journal Article

XIAP loss triggers RIPK3- and caspase-8-driven IL-1β activation and cell death as a consequence of TLR-MyD88-induced cIAP1-TRAF2 degradation

Lawlor, Kate E., Feltham, Rebecca, Yabal, Monica, Conos, Stephanie A., Chen, Kaiwen W., Ziehe, Stephanie, Grass, Carina, Zhan, Yifan, Nguyen, Tan A., Hall, Cathrine, Vince, Angelina J., Chatfield, Simon M., D'Silva, Damian B., Pang, Kenneth C., Schroder, Kate, Silke, John, Vaux, David L., Jost, Philipp J. and Vince, James E. (2017). XIAP loss triggers RIPK3- and caspase-8-driven IL-1β activation and cell death as a consequence of TLR-MyD88-induced cIAP1-TRAF2 degradation. Cell Reports, 20 (3), 668-682. doi: 10.1016/j.celrep.2017.06.073

XIAP loss triggers RIPK3- and caspase-8-driven IL-1β activation and cell death as a consequence of TLR-MyD88-induced cIAP1-TRAF2 degradation

2017

Other Outputs

Novel compounds and uses

O'Neill, L. A., Coll, R. C., Cooper, M. A., Robertson, A. A. B., Schroder, K., MacLeod, A. M. and Miller, D. J. (2017). Novel compounds and uses. PCT/IB2017/053059.

Novel compounds and uses

2017

Journal Article

NLRP3 inflammasome blockade reduces liver inflammation and fibrosis in experimental NASH in mice

Mridha, Auvro R., Wree, Alexander, Robertson, Avril A. B., Yeh, Matthew M., Johnson, Casey D., Van Rooyen, Derrick M., Haczeyni, Fahrettin, Teoh, Narci C. -H., Savard, Christopher, Ioannou, George N., Masters, Seth L., Schroder, Kate, Cooper, Matthew A., Feldstein, Ariel E. and Farrell, Geoffrey C. (2017). NLRP3 inflammasome blockade reduces liver inflammation and fibrosis in experimental NASH in mice. Journal of Hepatology, 66 (5), 1037-1046. doi: 10.1016/j.jhep.2017.01.022

NLRP3 inflammasome blockade reduces liver inflammation and fibrosis in experimental NASH in mice

2017

Journal Article

Active MLKL triggers the NLRP3 inflammasome in a cell intrinsic manner

Conos, Stephanie A. , Chen, Kaiwen W. , De Nardo, Dominic , Hara, Hideki , Whitehead, Lachlan , Núñez, Gabriel , Masters, Seth L. , Murphy, James M. , Schroder, Kate , Vaux, David L. , Lawlor, Kate E. , Lindqvist, Lisa M. and Vince, James E. (2017). Active MLKL triggers the NLRP3 inflammasome in a cell intrinsic manner. Proceedings of the National Academy of Sciences of the United States of America (PNAS), 114 (6), E961-E969. doi: 10.1073/pnas.1613305114

Active MLKL triggers the NLRP3 inflammasome in a cell intrinsic manner

2016

Journal Article

Role of NLRP3 inflammasome in a model of acute burn-induced pain

Deuis, Jennifer R., Yin, Kathleen, Cooper, Matthew A., Schroder, Kate and Vetter, Irina (2016). Role of NLRP3 inflammasome in a model of acute burn-induced pain. Burns, 43 (2), 304-309. doi: 10.1016/j.burns.2016.09.001

Role of NLRP3 inflammasome in a model of acute burn-induced pain

2016

Journal Article

Salmonella-induced inflammasome activation in humans

Bierschenk, Damien, Boucher, Dave and Schroder, Kate (2016). Salmonella-induced inflammasome activation in humans. Molecular Immunology, 86, 38-43. doi: 10.1016/j.molimm.2016.11.009

Salmonella-induced inflammasome activation in humans

2016

Journal Article

K+ efflux-independent NLRP3 inflammasome activation by small molecules targeting mitochondria

Groß, Christina J., Mishra, Ritu, Schneider, Katharina S., Médard, Guillaume, Wettmarshausen, Jennifer, Dittlein, Daniela C., Shi, Hexin, Gorka, Oliver, Koenig, Paul-Albert, Fromm, Stephan, Magnani, Giovanni, Ćiković, Tamara, Hartjes, Lara, Smollich, Joachim, Robertson, Avril A. B., Cooper, Matthew A., Schmidt-Supprian, Marc, Schuster, Michael, Schroder, Kate, Broz, Petr, Traidl-Hoffmann, Claudia, Beutler, Bruce, Kuster, Bernhard, Ruland, Jürgen, Schneider, Sabine, Perocchi, Fabiana and Groß, Olaf (2016). K+ efflux-independent NLRP3 inflammasome activation by small molecules targeting mitochondria. Immunity, 45 (4), 761-773. doi: 10.1016/j.immuni.2016.08.010

K+ efflux-independent NLRP3 inflammasome activation by small molecules targeting mitochondria

2016

Other Outputs

Sulfonylureas and related compounds and use of the same

O'Neill, Luke, Coll, Rebecca, Cooper, Matt, Robertson, Avril and Schroder, Kate (2016). Sulfonylureas and related compounds and use of the same. WO2016131098.

Sulfonylureas and related compounds and use of the same

2016

Journal Article

IL-1 contributes to the anti-cancer efficacy of ingenol mebutate

Le, Thuy T., Skak, Kresten, Schroder, Kate, Schroder, Wayne A., Boyle, Glen M., Pierce, Carly J. and Suhrbier, Andreas (2016). IL-1 contributes to the anti-cancer efficacy of ingenol mebutate. PLoS One, 11 (4) e0153975, e0153975. doi: 10.1371/journal.pone.0153975

IL-1 contributes to the anti-cancer efficacy of ingenol mebutate

2016

Journal Article

Questions and Controversies in innate immune research: What is the physiological role of NLRP3?

Coll, R. C., O'Neill, L. A. J. and Schroder, K. (2016). Questions and Controversies in innate immune research: What is the physiological role of NLRP3?. Cell Death Discovery, 2 (Art No.: 16019) 16019, 16019. doi: 10.1038/cddiscovery.2016.19

Questions and Controversies in innate immune research: What is the physiological role of NLRP3?

2016

Journal Article

The murine neutrophil NLRP3 inflammasome is activated by soluble but not particulate or crystalline agonists

Chen, Kaiwen W., Bezbradica, Jelena S., Gross, Christina J., Wall, Adam A., Sweet, Matthew J., Stow, Jennifer L. and Schroder, Kate (2016). The murine neutrophil NLRP3 inflammasome is activated by soluble but not particulate or crystalline agonists. European Journal of Immunology, 46 (4), 1004-1010. doi: 10.1002/eji.201545943

The murine neutrophil NLRP3 inflammasome is activated by soluble but not particulate or crystalline agonists

2016

Journal Article

Familial auto inflammation with neutrophilic dermatosis reveals a novel regulatory mechanism of pyrin activation

Masters, Seth L., Lagou, Vasiliki, Jéru, Isabelle, Baker, Paul J., Van Eyck, Lien, Parry, David A., Lawless, Dylan, De Nardo, Dominic, Garcia-Perez, Josselyn E., Dagley, Laura F., Holley, Caroline L., Dooley, James, Moghaddas, Fiona, Pasciuto, Emanuela, Jeandel, Pierre-Yves, Sciot, Raf, Lyras, Dena, Webb, Andrew I., Nicholson, Sandra E., De Somer, Lien, van Nieuwenhove, Erika, Ruuth-Praz, Julia, Copin, Bruno, Cochet, Emmanuelle, Medlej-Hashim, Myrna, Megarbane, Andre, Schroder, Kate, Savic, Sinisa, Goris, An ... Liston, Adrian (2016). Familial auto inflammation with neutrophilic dermatosis reveals a novel regulatory mechanism of pyrin activation. Science Translational Medicine, 8 (332) 332ra45, 1-9. doi: 10.1126/scitranslmed.aaf1471

Familial auto inflammation with neutrophilic dermatosis reveals a novel regulatory mechanism of pyrin activation

2016

Journal Article

Sterile signals generate weaker and delayed macrophage NLRP3 inflammasome responses relative to microbial signals

Bezbradica, Jelena S., Coll, Rebecca C. and Schroder, Kate (2016). Sterile signals generate weaker and delayed macrophage NLRP3 inflammasome responses relative to microbial signals. Cellular and Molecular Immunology, 1-9. doi: 10.1038/cmi.2016.11

Sterile signals generate weaker and delayed macrophage NLRP3 inflammasome responses relative to microbial signals

2016

Journal Article

Salmonella employs multiple mechanisms to subvert the TLR-inducible zinc-mediated antimicrobial response of human macrophages

Kapetanovic, Ronan, Bokil, Nilesh J., Achard, Maud E. S., Ong, Cheryl-lynn Y, Peters, Kate M., Stocks, Claudia J., Phan, Minh-Duy, Monteleone, Mercedes, Schroder, Kate, Irvine, Katharine M., Saunders, Bernadette M., Walker, Mark J., Stacey, Katryn J., McEwan, Alastair G., Schembri, Mark A. and Sweet, Matthew J. (2016). Salmonella employs multiple mechanisms to subvert the TLR-inducible zinc-mediated antimicrobial response of human macrophages. The FASEB Journal, 30 (5), 1901-1912. doi: 10.1096/fj.201500061

Salmonella employs multiple mechanisms to subvert the TLR-inducible zinc-mediated antimicrobial response of human macrophages

2016

Journal Article

The E3 ubiquitin ligase RNF144B is LPS-inducible in human but not mouse macrophages, and promotes inducible IL-1β expression

Ariffin, Juliana K., Kapetanovic, Ronan, Schaale, Kolja, Gatica-Andrades, Marcela, Blumenthal, Antje, Schroder, Kate and Sweet, Matthew J. (2016). The E3 ubiquitin ligase RNF144B is LPS-inducible in human but not mouse macrophages, and promotes inducible IL-1β expression. Journal of Leukocyte Biology, 100 (1), 155-161. doi: 10.1189/jlb.2AB0815-339R

The E3 ubiquitin ligase RNF144B is LPS-inducible in human but not mouse macrophages, and promotes inducible IL-1β expression

2016

Journal Article

NLRP12 is a neutrophil-specific, negative regulator of in vitro cell migration but does not modulate LPS- or infection-induced NF-κB or ERK signalling

Zamoshnikova, Alina, Grob, Christina J., Schuster, Steffen, Chen, Kaiwen W., Wilson, Anne, Tacchini-Cottier, Fabienne and Schroder, Kate (2016). NLRP12 is a neutrophil-specific, negative regulator of in vitro cell migration but does not modulate LPS- or infection-induced NF-κB or ERK signalling. Immunobiology, 221 (2), 341-346. doi: 10.1016/j.imbio.2015.10.001

NLRP12 is a neutrophil-specific, negative regulator of in vitro cell migration but does not modulate LPS- or infection-induced NF-κB or ERK signalling

2016

Book Chapter

Assessment of inflammasome formation by flow cytometry

Sester, David P., Zamoshnikova, Alina, Thygesen, Sara J., Vajjhala, Parimala R., Cridland, Simon O., Schroder, Kate and Stacey, Katryn J. (2016). Assessment of inflammasome formation by flow cytometry. Current protocols in immunology. (pp. 14.40.1-14.40.29) edited by Coligan, John E., Bierer, Barbara, Margulies, David H., Shevach, Ethan M. and Strober, Warren. Hoboken, NJ United States: John Wiley & Sons. doi: 10.1002/cpim.13

Assessment of inflammasome formation by flow cytometry

2016

Journal Article

Strain- and host species-specific inflammasome activation, IL-1β release, and cell death in macrophages infected with uropathogenic Escherichia coli.

Schaale, K., Peters, K. M., Murthy, A. M., Fritzsche, A. K., Phan, M.-D., Totsika, M., Robertson, A. A. B., Nichols, K. B., Cooper, M. A., Stacey, K. J., Ulett, G. C., Schroder, K., Schembri, M. A. and Sweet, M. J. (2016). Strain- and host species-specific inflammasome activation, IL-1β release, and cell death in macrophages infected with uropathogenic Escherichia coli.. Mucosal Immunology, 9 (1), 124-136. doi: 10.1038/mi.2015.44

Strain- and host species-specific inflammasome activation, IL-1β release, and cell death in macrophages infected with uropathogenic Escherichia coli.

2016

Conference Publication

Molecular arrangement and activation of procaspases-1 and-8 at inflammasomes

Vajjhala, P., Lu, A., Brown, D., Sagulenko, V, Schroder, K., Stow, J., Wu, H. and Stacey, K. (2016). Molecular arrangement and activation of procaspases-1 and-8 at inflammasomes. ICI 2016 International Congress of Immunology, Melbourne, Australia, 21-26 August 2016. Weinheim, Germany: Wiley.

Molecular arrangement and activation of procaspases-1 and-8 at inflammasomes

2015

Journal Article

The inflammasome adaptor ASC induces procaspase-8 death effector domain filaments

Vajjhala, Parimala R., Lu, Alvin, Brown, Darren L., Pang, Siew Wai, Sagulenko, Vitaliya, Sester, David P., Cridland, Simon O., Hill, Justine M., Schroder, Kate, Stow, Jennifer L., Wu, Hao and Stacey, Katryn J. (2015). The inflammasome adaptor ASC induces procaspase-8 death effector domain filaments. Journal of Biological Chemistry, 290 (49), 29217-29230. doi: 10.1074/jbc.M115.687731

The inflammasome adaptor ASC induces procaspase-8 death effector domain filaments

Funding

Current funding

  • 2024 - 2025
    Hope on the horizon - Harnessing inflammation as a novel diagnostic for chronic liver disease (2024 MSHRSS Co-funded Collaboration Grant led by MSH)
    Metro South Health Research Support Scheme Project Grant
    Open grant
  • 2023 - 2026
    Pyroptotic macrophages posthumously sculpt immune responses
    ARC Discovery Projects
    Open grant
  • 2022 - 2025
    Nuclear alarmins escalate tissue immune responses
    ARC Discovery Projects
    Open grant
  • 2022 - 2026
    Inflammasome inhibitors as new first-in-class anti-inflammatory therapies
    NHMRC Investigator Grants
    Open grant
  • 2022 - 2026
    Mining the host-pathogen interface to deliver a drug pipeline for treating intractable and emerging infections
    NHMRC Synergy Grants
    Open grant

Past funding

  • 2023 - 2024
    Elucidating Cardiolipin and Immune Dysfunction in Barth Syndrome
    The Barth Syndrome Foundation
    Open grant
  • 2021 - 2023
    Accelerating the diagnosis of children with autoinflammatory diseases
    Specific Donations Research Grant
    Open grant
  • 2020 - 2022
    A novel mechanism of host defence via macrophage extracellular traps
    ARC Discovery Projects
    Open grant
  • 2019 - 2021
    Developing treatments for vincristine-induced neuropathy
    The Kid's Cancer Project
    Open grant
  • 2019 - 2023
    Pathogenic functions for the NLRP3 inflammasome in Alzheimer's Disease
    The Yulgilbar Foundation
    Open grant
  • 2019 - 2022
    Molecular determinants of inflammatory caspase activity upon inflammasomes
    ARC Discovery Projects
    Open grant
  • 2019
    Advanced Brightfield and Fluorescent High Speed and Throughput Slide Scanner for biological, medical, materials science, and agricultural applications
    UQ Major Equipment and Infrastructure
    Open grant
  • 2019
    In vivo imaging system for tracking inflammation, infection, cancer, pain and bioactive molecules
    UQ Major Equipment and Infrastructure
    Open grant
  • 2019 - 2021
    PyroNETosis: a new mechanism of host defence
    NHMRC Project Grant
    Open grant
  • 2018
    Epifluorescent and live-cell imaging microscopes for the investigation of host-pathogen interactions and for molecular and cellular biology
    UQ Major Equipment and Infrastructure
    Open grant
  • 2018 - 2021
    Extinguishing the fire: inflammasome inhibition
    NHMRC Career Development Fellowship
    Open grant
  • 2017 - 2024
    ACRF Cancer Ultrastructure and Function Facility
    Australian Cancer Research Foundation
    Open grant
  • 2017 - 2019
    A novel mechanism for IL-1B secretion
    NHMRC Project Grant
    Open grant
  • 2017 - 2019
    Inflammatory pathways to liver fibrosis in non-alcoholic and alcoholic steatohepatitis: reversal by NLRP3 inhibitors (NHMRC Project Grant administered by ANU)
    Australian National University
    Open grant
  • 2016 - 2018
    Pharmacological Targeting of Proinflammatory Kinase Signalling in Parkinson's disease
    The Michael J Fox Foundation for Parkinsons Research
    Open grant
  • 2016 - 2020
    Blocking inflammasome-induced neuroinflammation in PD with a potent, orally available small molecule
    The Michael J Fox Foundation Therapeutic Pipeline Program
    Open grant
  • 2016 - 2019
    A molecular timer for inflammation and cell death
    ARC Discovery Projects
    Open grant
  • 2016 - 2018
    Autophagic suppression of ASC inflammasomes
    NHMRC Project Grant
    Open grant
  • 2015 - 2017
    Pharmacological targeting of the NLRP3 inflammasome in pre-clinical models of Parkinson's disease using a potent orally active inhibitor
    The Michael J Fox Foundation for Parkinsons Research
    Open grant
  • 2015 - 2017
    Inhibitors of NLRP3 activation for treatment of inflammatory CNS diseases
    NHMRC Project Grant
    Open grant
  • 2015
    Murine behavioural phenotyping facility
    UQ Major Equipment and Infrastructure
    Open grant
  • 2015 - 2016
    Therapeutic targeting of the NLRP3 inflammasome using a potent and orally active inhibitor in experimental MND
    Motor Neurone Disease Research Institute of Australia Inc
    Open grant
  • 2014 - 2018
    Inflammasomes: molecular drivers of anti-microbial defence
    ARC Future Fellowships
    Open grant
  • 2014 - 2016
    Microbial evasion of a novel inflammasome by Salmonella
    NHMRC Project Grant
    Open grant
  • 2014
    Pinpointing the initiation of immune responses
    UQ Foundation Research Excellence Awards - DVC(R) Funding
    Open grant
  • 2013 - 2016
    Caspase 8 apoptotic signalling induced by the inflammasome
    NHMRC Project Grant
    Open grant
  • 2013 - 2015
    Smart Futures Fellowship (Mid): Development of strategies to predict type 2 diabetes risk, and prevent diabetes onset in at-risk Queensland children
    Queensland Government Smart Futures Fellowships
    Open grant
  • 2012 - 2014
    Inflammasome function in neutrophils
    NHMRC Project Grant
    Open grant
  • 2011 - 2012
    NHMRC Training Fellowship (CJ Martin): Inflammasome function in gastrointestinal immunity and inflammation
    NHMRC Training (Postdoctoral) Fellowship
    Open grant
  • 2005 - 2008
    Human macrophage transcriptional network
    Riken Genomic Sciences Center
    Open grant

Supervision

Availability

Professor Kate Schroder is:
Available for supervision

Before you email them, read our advice on how to contact a supervisor.

Available projects

  • Student projects

    Expressions of interest from prospective postgraduate students are welcome at any time. For information on future research higher degree projects, please email K.Schroder@imb.uq.edu.au with the following: (1) CV, including a summary of academic qualifications, work and research experience, and publication list; (2) studies report for undergraduate and honours degree(s); and (3) a letter of motivation outlining your research interests.

Supervision history

Current supervision

Completed supervision

Media

Enquiries

Contact Professor Kate Schroder directly for media enquiries about:

  • Alzheimer's disease
  • arthritis
  • cancer
  • candida
  • caspase
  • cell biology
  • cytokine
  • diabetes
  • gout
  • hereditary disease
  • immune system
  • inerluekin
  • infection
  • infectious disease
  • inflammasome
  • inflammation
  • inflammatory disease
  • innate immunity
  • macrophage
  • myeloid
  • neutrophil
  • nod-like receptor
  • pyroptosis
  • salmonella
  • toll-like receptor

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